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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 4
1990 3
1991 5
1992 5
1993 2
1994 1
1995 1
1996 6
1997 4
1998 3
2000 1
2001 4
2002 5
2003 5
2004 2
2005 10
2006 10
2007 7
2008 10
2009 7
2010 9
2011 9
2012 11
2013 14
2014 8
2015 8
2016 15
2017 11
2018 10
2019 9
2020 8
2021 16
2022 9
2023 6
2024 5

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214 results

Results by year

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Page 1
Spectrum of mutations in Gitelman syndrome.
Vargas-Poussou R, Dahan K, Kahila D, Venisse A, Riveira-Munoz E, Debaix H, Grisart B, Bridoux F, Unwin R, Moulin B, Haymann JP, Vantyghem MC, Rigothier C, Dussol B, Godin M, Nivet H, Dubourg L, Tack I, Gimenez-Roqueplo AP, Houillier P, Blanchard A, Devuyst O, Jeunemaitre X. Vargas-Poussou R, et al. Among authors: houillier p. J Am Soc Nephrol. 2011 Apr;22(4):693-703. doi: 10.1681/ASN.2010090907. Epub 2011 Mar 17. J Am Soc Nephrol. 2011. PMID: 21415153 Free PMC article.
Global guidance for the recognition, diagnosis, and management of tumor-induced osteomalacia.
Jan de Beur SM, Minisola S, Xia WB, Abrahamsen B, Body JJ, Brandi ML, Clifton-Bligh R, Collins M, Florenzano P, Houillier P, Imanishi Y, Imel EA, Khan AA, Zillikens MC, Fukumoto S. Jan de Beur SM, et al. Among authors: houillier p. J Intern Med. 2023 Mar;293(3):309-328. doi: 10.1111/joim.13593. Epub 2022 Dec 13. J Intern Med. 2023. PMID: 36511653 Free PMC article. Review.
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy.
Schlingmann KP, Jouret F, Shen K, Nigam A, Arjona FJ, Dafinger C, Houillier P, Jones DP, Kleinerüschkamp F, Oh J, Godefroid N, Eltan M, Güran T, Burtey S, Parotte MC, König J, Braun A, Bos C, Ibars Serra M, Rehmann H, Zwartkruis FJT, Renkema KY, Klingel K, Schulze-Bahr E, Schermer B, Bergmann C, Altmüller J, Thiele H, Beck BB, Dahan K, Sabatini D, Liebau MC, Vargas-Poussou R, Knoers NVAM, Konrad M, de Baaij JHF. Schlingmann KP, et al. Among authors: houillier p. J Am Soc Nephrol. 2021 Nov;32(11):2885-2899. doi: 10.1681/ASN.2021030333. Epub 2021 Oct 4. J Am Soc Nephrol. 2021. PMID: 34607910 Free PMC article.
High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.
Hureaux M, Ashton E, Dahan K, Houillier P, Blanchard A, Cormier C, Koumakis E, Iancu D, Belge H, Hilbert P, Rotthier A, Del Favero J, Schaefer F, Kleta R, Bockenhauer D, Jeunemaitre X, Devuyst O, Walsh SB, Vargas-Poussou R. Hureaux M, et al. Among authors: houillier p. Kidney Int. 2019 Dec;96(6):1408-1416. doi: 10.1016/j.kint.2019.08.027. Epub 2019 Sep 16. Kidney Int. 2019. PMID: 31672324 Free article.
Etiology and Pathophysiology of Hypoparathyroidism: A Narrative Review.
Pasieka JL, Wentworth K, Yeo CT, Cremers S, Dempster D, Fukumoto S, Goswami R, Houillier P, Levine MA, Pasternak JD, Perrier ND, Sitges-Serra A, Shoback DM. Pasieka JL, et al. Among authors: houillier p. J Bone Miner Res. 2022 Dec;37(12):2586-2601. doi: 10.1002/jbmr.4714. Epub 2022 Nov 23. J Bone Miner Res. 2022. PMID: 36153665 Free PMC article.
[Primary hyperparathyroidism].
Maruani G, Cornière N, Nicolet L, Baron S, Courbebaisse M, Renaud S, Houillier P. Maruani G, et al. Among authors: houillier p. Rev Med Interne. 2013 Oct;34(10):605-13. doi: 10.1016/j.revmed.2012.10.369. Epub 2012 Nov 26. Rev Med Interne. 2013. PMID: 23195909 Review. French.
Claudins in Renal Physiology and Pathology.
Prot-Bertoye C, Houillier P. Prot-Bertoye C, et al. Among authors: houillier p. Genes (Basel). 2020 Mar 10;11(3):290. doi: 10.3390/genes11030290. Genes (Basel). 2020. PMID: 32164158 Free PMC article. Review.
Calcium-sensing in the kidney.
Houillier P. Houillier P. Curr Opin Nephrol Hypertens. 2013 Sep;22(5):566-71. doi: 10.1097/MNH.0b013e328363ff5f. Curr Opin Nephrol Hypertens. 2013. PMID: 23917029 Review.
Calcium Sensing in the Renal Tubule.
Toka HR, Pollak MR, Houillier P. Toka HR, et al. Among authors: houillier p. Physiology (Bethesda). 2015 Jul;30(4):317-26. doi: 10.1152/physiol.00042.2014. Physiology (Bethesda). 2015. PMID: 26136545 Free article. Review.
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.
Viering D, Schlingmann KP, Hureaux M, Nijenhuis T, Mallett A, Chan MMY, van Beek A, van Eerde AM, Coulibaly JM, Vallet M, Decramer S, Pelletier S, Klaus G, Kömhoff M, Beetz R, Patel C, Shenoy M, Steenbergen EJ, Anderson G, Bongers EMHF, Bergmann C, Panneman D, Rodenburg RJ, Kleta R, Houillier P, Konrad M, Vargas-Poussou R, Knoers NVAM, Bockenhauer D, de Baaij JHF; Genomics England Research Consortium. Viering D, et al. Among authors: houillier p. J Am Soc Nephrol. 2022 Feb;33(2):305-325. doi: 10.1681/ASN.2021050596. Epub 2021 Oct 4. J Am Soc Nephrol. 2022. PMID: 34607911 Free PMC article.
214 results